PathFinder NXT®

28 catalogue numbers from 3512-130, listed by Zimmer Spine, Inc., United States, under Orthosis, Spondylolisthesis Spinal Fixation. 13 manufacturers in China are registered for this product code.

Registry build 21.09.26
13manufacturers in China registered for this device type
28catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Jiangsu (7), Shanghai (2), Shandong (2). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code MNH
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
APS Materials Suzhou Suzhou Jiangsu Contract manufacturer 18
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Johnson & Johnson Medical (Depuy – Suzhou) Ltd. Suzhou Jiangsu Manufacturer 34
Double Medical Technology Inc. Xiamen Fujian Contract manufacturer 14
Suzhou Kangli Orthopaedics Instrument Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 11
Changzhou Yonghua Medical Instruments Co., Ltd. Changzhou Jiangsu Manufacturer 8
Jiangsu Ideal Medical Science & Technology Co., Ltd. Zhangjiagang Jiangsu Contract manufacturer 7

Showing 12 of 13. All 13 manufacturers in China registered for Orthosis, Spondylolisthesis Spinal Fixation

Record

Regulatory record for PathFinder NXT®
Listed by Zimmer Spine, Inc., United States
FDA product code MNH
Device type Orthosis, Spondylolisthesis Spinal Fixation
Device class Class 2
Regulation 21 CFR 888.3070
Record published 2015-09-24
Record revised 2025-01-03 (version 10)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Sizes Outer diameter 4.5 to 7.5 mm; length 30 to 190 mm

Catalogue Numbers

Catalogue numbers for PathFinder NXT®
Catalogue number Size Status
3512-130 Outer Diameter 5.5 mm In distribution
3570-10 In distribution
3512-160 Length 160 mm In distribution
3552-150 In distribution
3512-120 Length 120 mm In distribution
3505-4535 Length 35 mm In distribution
3510-070 Outer Diameter 5.5 mm In distribution
3554-100 In distribution
3552-170 In distribution
3512-190 Length 190 mm In distribution
3505-5535 Outer Diameter 5.5 mm In distribution
3557-0001 In distribution
3568-10 In distribution
3505-7550 Outer Diameter 7.5 mm In distribution
3557-3000 In distribution
3505-6550 Length 50 mm In distribution
3552-260 In distribution
3510-060 Outer Diameter 5.5 mm In distribution
3505-7560 Length 60 mm In distribution
3554-040 In distribution
3505-5540 Outer Diameter 5.5 mm In distribution
3510-090 Outer Diameter 5.5 mm In distribution
3510-055 Length 55 mm In distribution
3510-080 Outer Diameter 5.5 mm In distribution
3505-4540 Length 40 mm In distribution
3510-085 Length 85 mm In distribution
3557-1300 In distribution
3505-7530 Outer Diameter 7.5 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 3,144
Anax™ 5.5 Spinal System CG MedTech Co., Ltd. 2,177
ReLine Nuvasive, Inc. 2,010
Creo Globus Medical, Inc. 1,619
Perfix™ Spinal System CG MedTech Co., Ltd. 1,476
Apex Spine System Spinecraft LLC 1,193
Olympic Astura Medical 1,173
Arsenal Alphatec Spine, Inc. 1,001
Revere Globus Medical, Inc. 997
Astra Spine System Spinecraft LLC 798
Apex-DL Spine System Spinecraft LLC 735
Zenius Spinal System Medyssey Co., Ltd. 712

Showing 12 of 811. All products under Orthosis, Spondylolisthesis Spinal Fixation

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K122592 2013-01-04

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer